The Cost-Effectiveness of Germline BReast CAncer Gene Testing in Metastatic Prostate Cancer Followed by Cascade Testing of First-Degree Relatives of Mutation Carriers

被引:1
|
作者
Teppala, Srinivas [1 ]
Scuffham, Paul [1 ]
Edmunds, Kim [2 ]
Roberts, Matthew J. [3 ,4 ]
Fairbairn, David [5 ]
Smith, David P. [6 ]
Horvath, Lisa [7 ,8 ,9 ]
Tuffaha, Haitham [2 ]
机构
[1] Griffith Univ, Ctr Appl Hlth Econ, Brisbane, Qld, Australia
[2] Univ Queensland, Ctr Business & Econ Hlth, Ctr Hlth Econ, Brisbane, Qld, Australia
[3] Univ Queensland, UQ Ctr Clin Res Roberts, Brisbane, Qld, Australia
[4] Royal Brisbane & Womens Hosp, Dept Urol, Brisbane, Qld, Australia
[5] Royal Brisbane & Womens Hosp, Dept Pathol, Brisbane, Qld, Australia
[6] Univ Sydney, Daffodil Ctr, Joint Canc Council NSW, Sydney, NSW, Australia
[7] Chris OBrien Lifehouse, Med Oncol, Camperdown, NSW, Australia
[8] Garvan Inst Med Res, Clin Prostate Canc Grp, Darlinghurst, NSW, Australia
[9] Univ Sydney, Fac Med & Hlth, Camperdown, NSW, Australia
基金
英国医学研究理事会;
关键词
BRCA; cascade testing; genetic testing; germline testing; metastatic prostate cancer; QUALITY-OF-LIFE; ACTIVE SURVEILLANCE; OVARIAN-CANCER; BRCA2; MEN; RISK; UTILITIES; OUTCOMES; WOMEN; UK;
D O I
10.1016/j.jval.2024.06.019
中图分类号
F [经济];
学科分类号
02 ;
摘要
Objectives: Patients with metastatic prostate cancer (mPCa) with BReast CAncer gene (BRCA) mutations benefit from targeted treatments (eg, olaparib). In addition, family members of affected patients have increased risk of hereditary cancers and benefit from early detection and prevention. International guidelines recommend genetic testing in mPCa; however, the value for money of testing patients with mPCa and cascade testing of blood-related family members has not been assessed. In this context, we evaluated the cost-effectiveness of germline BRCA testing in patients with mPCa followed by cascade testing of first-degree relatives (FDRs) of mutation carriers. Methods: We conducted a cost-utility analysis of germline BRCA testing using 2 scenarios: (1) testing patients with mPCa only and (2) testing patients with mPCa and FDRs of those who test positive. A semi-Markov multi-health-state transition model was constructed using a lifetime time horizon. The analyses were performed from an Australian payer perspective. Decision uncertainty was characterized using probabilistic analyses. Results: Compared with no testing, BRCA testing in mPCa was associated with an incremental cost of AU$3731 and a gain of 0.014 quality-adjusted life-years (QALYs), resulting in an incremental cost-effectiveness ratio of AU$265 942/QALY. Extending testing to FDRs of variant-positive patients resulted in an incremental cost-effectiveness ratio of AU$16 392/QALY. Probability of cost-effectiveness at a willingness-to-pay of AU$75 000/QALY was 0% in the standalone mPCa analysis and 100% in the cascade testing analysis. Conclusion: BRCA testing when performed as a standalone strategy in patients with mPCa may not be cost-effective but demonstrates significant value for money after the inclusion of cascade testing of FDRs of mutation carriers.
引用
收藏
页码:1515 / 1527
页数:13
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